A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148882



Internal ID19196698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:152764883..152782077hg38UCSC Ensembl
OuterchrX:151933399..151950600hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3817195
hg1917202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997670
SamplesKWB1
Known GenesMAGEA3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148882
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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